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Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes

The creation of new functional molecules is a central task in chemical synthesis. Herein, we report the synthesis of a new type of fluorophore, bisbenzo[f]isoindolylidenes, from easily accessible dipropargyl benzenesulfonamides. Wavelength-tunable fluorophores emitting strong fluorescence of green t...

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Detalles Bibliográficos
Autores principales: Ye, Changqing, Huang, Rui, Chiou, Mong-Feng, Wang, Bo, Li, Daliang, Bao, Hongli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664550/
https://www.ncbi.nlm.nih.gov/pubmed/38023512
http://dx.doi.org/10.1039/d3sc04445a
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author Ye, Changqing
Huang, Rui
Chiou, Mong-Feng
Wang, Bo
Li, Daliang
Bao, Hongli
author_facet Ye, Changqing
Huang, Rui
Chiou, Mong-Feng
Wang, Bo
Li, Daliang
Bao, Hongli
author_sort Ye, Changqing
collection PubMed
description The creation of new functional molecules is a central task in chemical synthesis. Herein, we report the synthesis of a new type of fluorophore, bisbenzo[f]isoindolylidenes, from easily accessible dipropargyl benzenesulfonamides. Wavelength-tunable fluorophores emitting strong fluorescence of green to red light were obtained in this reaction. Late-stage modifications and incorporation of bioactive molecules into these fluorophores give rise to potential applications in biological studies. Detailed computational and experimental studies were conducted to elucidate the mechanism, and suggest a reaction sequence involving Garratt–Braverman type cyclization, isomerization, fragmentation, dimerization and oxidation.
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spelling pubmed-106645502023-11-02 Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes Ye, Changqing Huang, Rui Chiou, Mong-Feng Wang, Bo Li, Daliang Bao, Hongli Chem Sci Chemistry The creation of new functional molecules is a central task in chemical synthesis. Herein, we report the synthesis of a new type of fluorophore, bisbenzo[f]isoindolylidenes, from easily accessible dipropargyl benzenesulfonamides. Wavelength-tunable fluorophores emitting strong fluorescence of green to red light were obtained in this reaction. Late-stage modifications and incorporation of bioactive molecules into these fluorophores give rise to potential applications in biological studies. Detailed computational and experimental studies were conducted to elucidate the mechanism, and suggest a reaction sequence involving Garratt–Braverman type cyclization, isomerization, fragmentation, dimerization and oxidation. The Royal Society of Chemistry 2023-11-02 /pmc/articles/PMC10664550/ /pubmed/38023512 http://dx.doi.org/10.1039/d3sc04445a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Ye, Changqing
Huang, Rui
Chiou, Mong-Feng
Wang, Bo
Li, Daliang
Bao, Hongli
Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes
title Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes
title_full Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes
title_fullStr Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes
title_full_unstemmed Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes
title_short Synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes
title_sort synthesis of a new fluorophore: wavelength-tunable bisbenzo[f]isoindolylidenes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664550/
https://www.ncbi.nlm.nih.gov/pubmed/38023512
http://dx.doi.org/10.1039/d3sc04445a
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